NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1376895 Query DataSets for GSM1376895
Status Public on Oct 31, 2014
Title Hypo-A2/12_control-4
Sample type RNA
 
Source name cell line HypoA-2/12, control, 24 h exposure, repliclate 4
Organism Mus musculus
Characteristics cell line: HypoA-2/12
cell type: hypothalamic neuronal cells
phenotype: serotonin unresponsive
Treatment protocol Cells were grown in monolayers to 90% confluency. Then medium was replaced by serum-free DMEM containing penicillin and streptomycin. After 4 hours, cells were exposed to serotonin.
Growth protocol Murine derived hypothalamic neuronal cell lines hypoE-46 and hypoA2/12 (CELLutions Biosystems Inc. Canada) were grown and maintained in DMEM supplemented with 10% heat-inactivated fetal calf serum, 100 units/ml penicillin and 100μg/ml streptomycin at 37 C under 5.0% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TrIzol (Life Technologies) according to manyfacturer's protocol. RNA integrity was checked on chip analysis (Agilent 2100 bioanalyzer, Agilent Technologies, Amsterdam, the Netherlands) according to the manufacturer's instructions. RNA was judged as suitable for array hybridization only if samples exhibited intact bands corresponding to the 18S and 28S ribosomal RNA subunits, and displayed no chromosomal peaks or RNA degradation products (RNA Integrity Number > 8.0).
Label biotin
Label protocol One hundred nanogram of RNA was used for whole transcript cDNA synthesis with the Ambion WT expression kit [catalog number 4411974] (Applied Biosystems/Life Technologies, Nieuwekerk a/d IJssel, The Netherlands).
 
Hybridization protocol Hybridization of 5.5μg labelled cDNA was done overnight for 17 hours, at 60 rpm, at 45ºC in a Hybridization Oven 640 (Affymetrix). The protocol was conducted as described in the Affymetrix Whole Transcript (WT) Sense Target Labeling Assay Manual, chapter 5 (P/N 701880, revision 5). Washing and staining of the arrays were done on an Affymetrix 450 fluidics station using the protocol FS450_0001, as described in the Affymetrix Whole Transcript (WT) Sense Target Labeling Assay Manual, chapter 5 (P/N 701880, revision 5).
Scan protocol Arrays were scanned on an Affymetrix GeneTitan instrument (Affymetrix, Santa Clara, CA).
Description G145_F05_16_177_m4.CEL (h177_control)
Data processing Expression estimates were calculated applying the RMA algorithm in the Bioconductor library 'Oligo' (v1.26.6).
 
Submission date Apr 30, 2014
Last update date Oct 31, 2014
Contact name Guido Hooiveld
E-mail(s) [email protected]
Organization name Wageningen University
Department Div. Human Nutrition & Health
Lab Nutrition, Metabolism & Genomics Group
Street address HELIX, Stippeneng 4
City Wageningen
ZIP/Postal code NL-6708WE
Country Netherlands
 
Platform ID GPL11533
Series (2)
GSE57189 Differences in food intake of tumour-bearing cachectic mice are associated with hypothalamic serotonin signalling [A358_GEO_hypocells]
GSE57190 Differences in food intake of tumour-bearing cachectic mice are associated with hypothalamic serotonin signalling

Data table header descriptions
ID_REF
VALUE RMA signal (as log2)

Data table
ID_REF VALUE
10338001 11.49039595
10338002 4.635457646
10338003 9.647013639
10338004 9.020649713
10338005 2.457209331
10338006 2.694708957
10338007 2.858528968
10338008 3.157900185
10338009 6.682672614
10338010 2.461340038
10338011 4.077372418
10338012 2.614597566
10338013 2.232098463
10338014 2.365476
10338015 2.296635709
10338016 5.535700259
10338017 12.67012525
10338018 5.068650492
10338019 3.689983939
10338020 6.424283708

Total number of rows: 35556

Table truncated, full table size 725 Kbytes.




Supplementary file Size Download File type/resource
GSM1376895_G145_F05_16_177_M4.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap